I am sorry that you and your father are facing this; and so close to the holidays. I will lift your family up in prayer for guidance, strength and comfort during this difficult time and a miracle if that is His will. 
I have now read your updates. God is amazing isn't He?
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When I woke up Thursday morning and took my temperature, it was NORMAL and I was feeling fine
I gave myself Friday to recover some more strength and then told Dad that I would go see Mom on Saturday and Sunday, so he could rest.
Like today when I went in around lunch time to feed her, I said "it sure would be a lot easier if you could use a straw" and she said "I can use a straw!"
Her liquids do have to be thickened to a honey like consistency and her meals are still pureed foods, but I think once we can get her dentures in she would be able to tolerate regular foods.
She has been to this facility 3 times in the past and they do excellent work, all the therapists know Mom very well, and Dad & I trust them with her care. At this point, we are just waiting for a bed to open up there and then they will transfer her.
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The only thing that the Discharge Planner said to us was that "English Oaks is not willing to take her because of the feeding tube, Parkinson's and *slight* dementia." Neither Dad or I can figure out why in just a matter of 4mths, that her Parkinson's & dementia is a problem. She was just released from there July 23rd and she was doing GREAT !!
that have been sent to Mom, Dad and myself
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Latest update on Mom is that she was moved to a Rehabilitation Facility yesterday afternoon, however English Oaks where we wanted her to go, would not take herThe only thing that the Discharge Planner said to us was that "English Oaks is not willing to take her because of the feeding tube, Parkinson's and *slight* dementia." Neither Dad or I can figure out why in just a matter of 4mths, that her Parkinson's & dementia is a problem. She was just released from there July 23rd and she was doing GREAT !!
So, the discharge planner had come up with 2 other alternatives and luckily I had a Dr appointment Thursday, because my primary Dr has been my Mom's Dr for about 20 yrs. He told me that the 2 alternatives were, and these are his words, "Death Traps!!!!!" So I went online and found another facility not to far away and asked that they check and see if they would take Mom. They did accept her, but again the bed vacancy problem came up.
I am NOT thrilled with this facility, but realize that it is better than the others they wanted to ship Mom off to. Dad and I have a meeting on Monday with the Physical Therapist, Occupational Therapist, Speech Therapist, and Dietitian to go over Mom's course of care. In the meantime, while Mom is at Evergreen, I intend to go to English Oaks and ask them WHY they would not accept Mom since she still has the same problems she did in July![]()
Mom is doing a lot more talking, holding her own drinking glass & drinking from it, and moving all her limbs on her own. So the next few steps will be to get her working on feeding herself and strengthening up her leg and arm muscles, so she can go back to using her walker.
Again, words can not express the gratitude of all the thoughts, prayers andthat have been sent to Mom, Dad and myself
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Lyn
But as far as the Doctor was concerned, their names might have well been that. Both places have had numerous deaths due to lack of staffing and the Medical Group, Sutter Gould, will NEVER place ANY of their patients in either facility.Thanks for the update.
Death Traps was actually the name of a place?
No, not at allBut as far as the Doctor was concerned, their names might have well been that. Both places have had numerous deaths due to lack of staffing and the Medical Group, Sutter Gould, will NEVER place ANY of their patients in either facility.
I was like.... people actually go to a place called that?
because I was so worried that she was not getting enough protein and even without her dentures and removing the top bun, she ate 95% of that burger
Yesterday I talked with the Speech Therapist and the head of Dietary and on Monday everyone is going to see how she does with eating this Big Mac and if she does okay, which she will, then we can start moving her towards a more normal diet. Tonight was a *huge* step for her at dinner time !! They got her into a wheelchair and took her down to the dining hall where she could feed herself, get out of the bed she has been basically living in, help relieve her back pain, and get a chance for her to talk with other patients. If she can continue to do this, it would help her development of muscle tone immensely, further develop her hand eye coordination and hopefully get her to understand that in order for her to get a "day pass" to come home for Christmas she has to be able to stand and transfer with help, from the car to a wheelchair.
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